Syringe Assembly Having a Rotatably Advanceable Plunger Rod

ABSTRACT

A syringe assembly for use as a pre-filled syringe is disclosed. The syringe assembly includes a syringe barrel defining a chamber and having a stopper disposed therein. A plunger rod includes an inner member engaged with a portion of the stopper and an outer member adapted for rotational advancement with respect to the inner member to axially displace the outer member with respect to the inner member. The plunger rod is transitionable from a collapsed position in which a portion of the inner member is nested within the outer member, to an extended position in which the same portion of the inner member extends outside the outer member. The inner member includes a radial extension and the outer member defines a helical track adapted to receive the radial extension therein.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to U.S. Provisional Patent ApplicationNo. 61/541,370 filed Sep. 30, 2011, the entire disclosure of which ishereby incorporated by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention is directed to a pre-filled syringe assemblyadapted for the dispensing and delivery of a fluid. More particularly,the present invention is directed to a pre-filled syringe assemblyhaving a rotatably advanceable plunger rod which results in a smallerpackaging footprint allowing for reduced storage space.

2. Description of Related Art

Syringe assemblies, and in particular hypodermic syringes, are wellknown in the medical field for dispensing fluids, such as medication. Aconventional syringe typically includes a syringe barrel with an openingat one end and a plunger mechanism disposed through the other end. Theplunger mechanism typically includes a plunger rod extending through thebarrel, with a plunger head or stopper at the end of the plunger rodwithin the barrel and with a finger flange at the other end of theplunger rod extending out of the barrel. In use, the plunger rod isretracted through the syringe barrel to fill the syringe barrel with afluid, such as a medication, with the plunger rod extending out from therear end of the syringe barrel. For delivery of the medication to apatient, the opening of the syringe barrel is adapted for fluidcommunication with a patient, such as through a hypodermic needle fittedat the front end of the syringe barrel or through a luer-type fittingextending from the front end of the syringe barrel for attachment with afluid line of a patient. Upon depression of the plunger rod, the plungerrod and stopper travel through the syringe barrel, thereby forcing thecontents of the syringe out through the opening at the front end fordelivery to the patient. Such an operation is well known in the medicalfield, and medical practitioners have become well accustomed to the useof such common fluid delivery procedures through standard syringes.

Conventional syringes are well known to be used in connection with avial of a medication, where the user draws the fluid into the syringeimmediately prior to injection and delivery of the fluid to the patient.Oftentimes, hypodermic syringes may be packaged as “pre-filled” devices,wherein the syringe is pre-filled with medication prior to beingpackaged and delivered to the end user. In this manner, there is no needfor the user to fill the device prior to injection, thereby saving timefor the end user and maintaining consistent volumes for delivery.

Pre-filled syringes and pre-filled metered dose syringes are oftenfilled with narcotics or other drugs at a production facility, packaged,and then shipped to a medical facility. Once at the facility, thesesyringes are often placed in controlled storage and/or locked cabinetsto reduce theft of the syringes themselves and/or theft of the contentsof these syringes. The space within these controlled storage locationsis often limited, thus there is a need for a syringe assembly that has asmaller packaging footprint to reduce the storage space required forcontaining this syringe. It is also desirable to produce syringes thatare uniform in terms of an outer surface shape to allow for stacking ofthe syringes within the storage cabinet. There is a further need forsyringe assemblies having a smaller packaging footprint that includetamper-evident indicators to allow medical practitioners to determinewhether the contents of a syringe assembly have been compromised.

SUMMARY OF THE INVENTION

In accordance with an embodiment of the present invention, a syringeassembly includes a syringe barrel having a first end, a second end, anda sidewall extending therebetween defining a chamber. A stopper isslideably disposed at least partially within the chamber. A plunger rodfor advancing the stopper includes an inner member engaged with aportion of the stopper and an outer member adapted for rotationaladvancement with respect to the inner member to axially displace theouter member with respect to the inner member. The plunger rod istransitionable from a collapsed position in which a portion of the innermember is nested within the outer member, to an extended position inwhich the same portion of the inner member extends outside the outermember.

In certain configurations, the inner member includes a radial extensionand the outer member defines a track adapted to receive the radialextension therein. The track may be at least partially helical about anouter surface of the outer member. The radial extension may remainsubstantially stationary during transition of the plunger rod from thecollapsed position to the extended position, and the outer member may berotated about the inner member to axially displace the outer member withrespect to the inner member. In certain configurations, the trackextends between a proximal end and a distal end, with the distal endincluding a restraint for locking the radial extension therein in theextended position. The stopper may remain substantially stationaryduring transition of the plunger rod from the collapsed position to theextended position. The syringe assembly may also include a medication ordrug disposed within the chamber.

In accordance with another embodiment of the present invention, aplunger rod assembly for use with a syringe assembly includes an innermember having a distal end configured for securement to a stopperdisposed within a syringe barrel. The plunger rod assembly also includesan outer member having an open portion configured for rotationaladvancement with respect to the inner member to axially displace theouter member with respect to the inner member. The plunger rod assemblyis transitionable from a collapsed position in which a portion of theinner member is nested within the outer member, to an extended positionin which the same portion of the inner member extends outside the outermember. The plunger rod assembly also includes a restraint configured tolimit axial advancement of the outer member with respect to the innermember in the extended position.

The restraint may be configured to limit axial advancement of the outermember in both the proximal direction and the distal direction in theextended position. The inner member may include a radial extension andthe outer member may define a track adapted to receive the radialextension therein. The track may be at least partially helical about anouter surface of the outer member. In certain configurations, the radialextension remains substantially stationary during transition of theplunger rod assembly from the collapsed position to the extendedposition. In other configurations, the track may extend between aproximal end and a distal end, with the distal end including a restraintfor locking the radial extension therein in the extended position.

In accordance with yet another embodiment of the present invention, asyringe assembly includes a syringe barrel having a first end, a secondend, and a sidewall extending therebetween defining a chamber. Thesyringe assembly also includes a stopper slideably disposed at leastpartially within the chamber, and a plunger rod. The plunger rodincludes an inner member engaged with a portion of the stopper andincludes a radial extension, and an outer member defining a trackadapted to receive the radial extension therein. Rotation of the outermember about the inner member axially displaces the track about theradial extension to transition the plunger rod from a collapsed positionin which a portion of the inner member is nested within the outermember, to an extended position in which the same portion of the innermember extends outside the outer member.

In certain configurations, the track is at least partially helical aboutan outer surface of the outer member. In other configurations, aninitial portion of the inner member and an initial portion of the outermember are disposed within the syringe barrel in the collapsed position.The initial portion of the outer member may, however, be external to thesyringe barrel in the extended position. Optionally, the track extendsbetween a proximal end and a distal end, with the distal end including arestraint for locking the radial extension therein in the extendedposition. In a further configuration, a medication or a drug is disposedwithin the chamber of the syringe barrel.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a perspective view of a syringe assembly including a rotatablyadvanceable plunger rod in an initial collapsed position in accordancewith an embodiment of the present invention.

FIG. 2 is a front view of the syringe assembly of FIG. 1 showing alocking tab of the plunger rod in a first position in the initialcollapsed position in accordance with an embodiment of the presentinvention.

FIG. 3 is a cross-sectional view of the syringe assembly of FIG. 1 takenalong line 3-3 of FIG. 2 in accordance with an embodiment of the presentinvention.

FIG. 4 is a front view of the syringe assembly of FIG. 1 showing thelocking tab of the plunger rod in the extended ready-to-use position inaccordance with an embodiment of the present invention.

FIG. 5 is a cross-sectional view of the syringe assembly of FIG. 1 takenalong line 5-5 of FIG. 4 in accordance with an embodiment of the presentinvention.

FIG. 6 is a front view of the syringe assembly of FIG. 1 showing thelocking tab of the plunger rod in the extended ready-to-use position andthe plunger rod deployed within the syringe barrel in accordance with anembodiment of the present invention.

FIG. 7 is a cross-sectional view of the syringe assembly of FIG. 1 takenalong line 7-7 of FIG. 6 in accordance with an embodiment of the presentinvention.

FIG. 8 is a cross-sectional view of the syringe assembly of FIG. 1 takenalong line 8-8 of FIG. 3 in accordance with an embodiment of the presentinvention.

FIG. 9 is a perspective view of the syringe assembly of FIG. 1 includinga tamper-evident packaging disposed thereover in accordance with anembodiment of the present invention.

FIG. 10 is a perspective view of the syringe assembly of FIG. 9 havingthe tamper-evident packaging partially removed therefrom in accordancewith an embodiment of the present invention.

DETAILED DESCRIPTION OF THE EMBODIMENTS

For purposes of the description hereinafter, the terms “upper”, “lower”,“right”, “left”, “vertical”, “horizontal”, “top”, “bottom”, “lateral”,“longitudinal”, and derivatives thereof shall relate to the invention asit is oriented in the drawing figures. However, it is to be understoodthat the invention may assume various alternative variations, exceptwhere expressly specified to the contrary. It is also to be understoodthat the specific devices illustrated in the attached drawings, anddescribed in the following specification, are simply exemplaryembodiments of the invention. Hence, specific dimensions and otherphysical characteristics related to the embodiments disclosed herein arenot to be considered as limiting.

Reference is now made to FIGS. 1-8, which depict a syringe assemblyaccording to an embodiment of the present invention, generally indicatedas 10, adapted for the dispensing and delivery of a fluid. FIGS. 9-10depict a packaging assembly, generally indicated as 200, and theoperational steps for removing the packaging assembly, which can be usedfor packaging the syringe assembly of the invention.

With particular reference to FIGS. 1-8, the syringe assembly 10 isintended for use for injection or infusion of fluid, such as amedication, directly into a patient, and is generally shown anddescribed for purposes of the present description as a hypodermicsyringe. Syringe assembly 10 is contemplated for use in connection witha needle such as by connecting syringe assembly 10 to a separate needleassembly (not shown), or alternatively for connection with a separateintravenous (IV) connection assembly (not shown).

The syringe assembly 10 includes a syringe barrel 12 having a first ordistal end 14, a second or proximal end 16, and a sidewall 18 extendingbetween the distal end 14 and proximal end 16 defining an interiorchamber 20 of the syringe barrel 12. A stopper 22 is slidably disposedwithin the chamber 20 of the syringe barrel 12. The syringe barrel 12may be in the general form of an elongated cylindrical barrel as isknown in the art for the general shape of a hypodermic syringe, althoughother forms for containing a fluid for delivery are also contemplated bythe present invention. Additionally, the syringe barrel 12 may be formedof glass, or may be injection molded from thermoplastic material such aspolypropylene and polyethylene according to techniques known to those ofordinary skill in the art, though it is to be appreciated that thesyringe barrel 12 may be made from other suitable materials andaccording to other applicable techniques. In certain configurations, thesyringe barrel 12 may include an outwardly extending flange 21 about atleast a portion of the proximal end 16. The flange 21 may be configuredfor easy grasping by a medical practitioner, as will be discussedherein.

As illustrated in FIG. 3, the distal end 14 of the syringe barrel 12terminates in a tip 24 having an outlet opening 26. The proximal end 16is generally open-ended, but is intended to be closed off to theexternal environment, via the stopper 22, as will be discussed herein.According to one non-limiting embodiment, as shown in FIG. 3, thesyringe assembly 10 can include a tip cap 28, an interface member 27interfacing between the tip cap 28 and the tip 24 of the syringe barrel12, and a plug 29, for sealing the outlet opening 26.

The syringe barrel 12 may include markings, such as graduations on thesidewall 18 thereof, for providing an indication as to the level oramount of fluid contained within the syringe barrel 12. Such markingsmay be provided on the external wall, the internal wall, or integrallyformed or otherwise within the wall of syringe barrel 12. Alternatively,or in addition thereto, the markings may provide a description of thecontents of the syringe, or other identifying information, as may beknown in the art.

As noted, distal end 14 of syringe barrel 12 includes an outlet opening26. The profile of outlet opening 26 may be adapted for engagement witha separate dispensing device, such as a needle assembly or IV connectionassembly, and therefore may include a mechanism for such engagement, forexample, a generally tapered luer tip, for engagement with a separatetapered luer mating surface (not shown) of such a separate device forattachment therewith. In addition, a mechanism for locking engagementtherebetween may also be provided, such as a luer collar or luer lockincluding interior threads. Such luer connections and luer lockingmechanisms are well known in the art.

All of the components of syringe assembly 10 may be constructed of anyknown material, and are desirably constructed of medical grade polymers.As stated above, the syringe assembly 10 is particularly useful as apre-filled syringe, and therefore may be provided for end use with afluid, such as a medication, contained within interior chamber 20 ofsyringe barrel 12, pre-filled by the manufacturer. In this manner,syringe assembly 10 can be manufactured, pre-filled with a medication,sterilized, and packaged in appropriate packaging for delivery, storage,and use by the end user, without the need for the end user to fill thesyringe with medication from a separate vial prior to use.

With continuing reference to FIGS. 1-8, the syringe assembly 10 includesa plunger rod assembly, generally indicated as 30, for controllingmovement of the stopper 22 slideably through the syringe barrel 12 toeither expel the syringe contents of a pre-filled type of syringeassembly 10 or, depending upon the desired use of the syringe assembly,to aspirate or withdraw a fluid into the syringe barrel 12. The plungerrod assembly 30 includes an inner member 32, as shown clearly in FIG. 3,including a distal end 34 secured to the stopper 22. In one embodiment,the distal end 34 of the inner member 32 may be secured to the stopper22 by way of a threaded engagement formed therebetween. In anotherembodiment, the distal end 34 of the inner member 32 may be co-formedwith the stopper 22, such as by a two-shot molding process. In still afurther embodiment, the distal end 34 of the inner member 32 may includean engagement plate 35 for receiving a portion of the stopper 22, suchas the flange 21 of the stopper 22, therewith. The inner member 32 maybe substantially cylindrical, although it is contemplated herein thatother shapes may also be included in the present invention.

In one configuration, the inner member 32 includes a radial extension 41extending radially outward from a portion of a sidewall 43 thereof. Theradial extension 41 may include a protrusion or other extensionextending outwardly from the sidewall 43.

The plunger rod assembly 30 also includes an outer member 36 which isadapted for rotational advancement with respect to the inner member 32.The outer member 36 may also be substantially cylindrical and mayinclude a hollow core 39, as shown in FIG. 5, although it iscontemplated herein that other shapes corresponding to the shape of theinner member 32 may also be included in the present invention. Asidewall 45 of the outer member 36 may include a track 47 disposedtherein extending from the external environment into the hollow core 39.In one configuration, the track extends within the sidewall 45 of theouter member 36 from a proximal end 49 of the outer member 36 to adistal end 51 of the outer member 36, as shown clearly in FIG. 4. In afurther configuration, the track is at least partially helicallydisposed within the sidewall 45 about an outer surface circumference ofthe outer member 36. The track 47 is dimensioned to receive the radialextension 41 of the inner member 32 therein.

The plunger rod assembly 30 can include a thumb press portion 64 or anyother type of well-known member, upon which a user can apply a distallydirected force to cause the plunger rod 30 to move the stopper 22,disposed within the syringe barrel 12, toward the distal end 14 of thesyringe barrel 12 to expel the syringe contents during operation of thesyringe assembly 10. This thumb press portion 64 can include a roughenedor serrated surface, as is known in the art, to provide a frictionalsurface for assisting the user in movement or actuation of the plungerrod. In one embodiment, the thumb press portion 64 may be disposedadjacent a proximal end 33 of the outer member 36.

The plunger rod assembly 30 is transitionable from a collapsed pre-useposition, as shown in FIGS. 1-3, to an extended ready-to-use position,as shown in FIGS. 4-5, to a used position, as shown in FIGS. 6-7.

In the collapsed pre-use position, as shown in FIGS. 1-3, at least aportion of the inner member 32 is nested within a portion of the outermember 36. In this configuration, at least a portion of the outer member36 includes an inner diameter D₁, as shown in FIG. 3, that is greaterthan the external diameter D₂ of at least a portion of the inner member32. Accordingly, outer member 36 is adapted to encompass at least aportion of inner member 32 in the collapsed pre-use position, such thatthe inner member 32 is nested within the outer member 36. In thecollapsed position, the stopper 22 may be disposed within the chamber 20at a substantially proximal location 57, and the inner member 32connected thereto may extend outwardly of the syringe barrel 12 withinthe hollow core 39 of the outer member 36. The radial extension 41 ofthe inner member 32 is disposed within the track 47 of the outer member36 at a first location adjacent the proximal end 49 of the outer member36.

In order to transition the plunger rod assembly 30 from the collapsedpre-use position to the extended ready-to-use position, a medicalpractitioner may rotate the outer member 36 about the inner member 32,such as by twisting the outer member 36 in the direction shown by arrowA of FIG. 4. The medical practitioner may grasp any portion of the outermember 36, such as the thumb press 64, to effectuate this rotation.Rotation of the outer member 36 with respect to the inner member 32causes the outer member 36 to be axially displaced from the inner member32 along a longitudinal axis L, as shown in FIG. 4, of the syringeassembly 10 from a distal orientation, as shown in FIGS. 1-3, to aproximal location, as shown in FIGS. 4-5. Once the plunger rod assembly30 is transitioned from the collapsed pre-use position to the extendedready-to-use position, at least a portion of the inner member 32 thatwas nested within the outer member 36 in the collapsed position, extendsoutside the outer member 36 in the extended position.

In one configuration, the inner member 32 is disposed in substantiallythe same position during the transition from the collapsed position tothe extended position. Specifically, the radial extension 41 of theinner member 32 may be disposed in substantially the same positionduring the transition from the collapsed position to the extendedposition. In a further configuration, the stopper 22 remainssubstantially stationary within the chamber 20 of the syringe barrel 12during transition of the plunger rod assembly 30 from the collapsedposition to the extended position. In a further configuration, aninitial portion 66 of the inner member 32 and an initial portion 68 ofthe outer member 36 are disposed within a portion of the syringe barrel12, as shown in FIG. 3, in the collapsed position. In the extendedposition, the initial portion 66 of the inner member 32 may remaindisposed within a portion of the syringe barrel 12, however, the initialportion 68 of the outer member 36 is disposed external to the syringebarrel 12.

As shown specifically in FIG. 4, the track 47 adjacent the distal end 51of the outer member 36 may include a restraint 70 for locking the radialextension 41 therein in the extended position. In one configuration, therestraint 70 may include a flattened recess 72 such that the radialextension 41 is secured within the recess 72 to prevent further axialmovement of the outer member 36 with respect to the inner member 32. Inone configuration, the restraint 70 is configured to limit further axialmovement of the outer member 36 with respect to the inner member 32 inthe proximal direction once the plunger rod assembly 30 has beentransitioned to the extended position. Accordingly, the application offorce in the direction of arrow B, as shown in FIG. 4, does not allowfor further displacement of the outer member 36 with respect to theinner member 32 once the plunger rod assembly 30 has been transitionedto the extended position. In still a further configuration, therestraint 70, shown in FIGS. 4-5, also limits relative movement betweenthe outer member 36 and the inner member 32 in the direction shown byarrow C of FIG. 6. Accordingly, once the plunger rod assembly 30 hasbeen transitioned to the extended position, as shown in FIGS. 4-5,application of a downward force in the direction of arrow C allows thelocked outer member 36 and inner member 32 to advance the stopper 22within the chamber 20, and does not allow for relative movement betweenthe outer member 36 and the inner member 32. FIG. 8 illustrates aportion of the track 47A adjacent the proximal end 49 of the outermember 36 for receiving the radial extension 41 in the collapsedposition, and a portion of the track 47B adjacent the distal end 51 ofthe outer member 36 receiving the radial extension 41 therein in theextended position.

With the plunger rod assembly 30 locked in position such that the outermember 36 and the inner member 32 move together, the syringe assembly 10may be transitioned to the used position, as shown in FIGS. 6-7. Duringtransition of the plunger rod assembly 30 from the extended position tothe used position, a medication or drug disposed within the chamber 20may be expelled therefrom by the advancement of the stopper 22, as isconventionally known.

It is noted herein that the radial extension 41 may extend outwardlyfrom the inner member 32 into a portion of the outer member 36 in anysuitable dimension that allows the combined plunger assembly 30 to bedeployed into the interior of the syringe barrel 12 without obstruction.

Reference is now made to FIGS. 9-10, which depict a packaging assembly,generally indicated as 200, and the sequential operational steps forremoving the packaging assembly 200 from the syringe assembly 10, inaccordance with an embodiment of the present invention. The packagingassembly 200 includes a molded cover 202 configured for placement abouta portion of the syringe barrel 12, the plunger rod assembly 30, and thetip cap 28. A tear tab 204 can be associated with one end 206 of themolded cover 202. The tear tab 204 is configured, such as by theinclusion of a frangible portion 207, to facilitate removal of themolded cover 202 from the syringe assembly 10, and can be positionedadjacent a top surface or thumb press 64 of the plunger rod assembly 30.The tear tab 204 can include a roughened or serrated surface, as isknown in the art, to provide a frictional surface for assisting the userin grasping of the tear tab 204. The cover 202 is configured forplacement about the syringe assembly 10 to constrain the plunger rodassembly 30 from inadvertent transition from the collapsed position tothe extended position and to prevent tampering of the syringe assembly10.

It can be appreciated that each of the syringe assemblies of the presentinvention includes a reduced footprint which is desirable in thepackaging of the syringe assemblies as it requires less packaging. Thisreduced footprint provides for syringe assemblies having consistentlysized profiles which allow for easy stacking and require less storagespace, both of these features being desirable in a controlled storageenvironment.

While specific embodiments of the invention have been described indetail, it will be appreciated by those skilled in the art that variousmodifications and alternatives to those details could be developed inlight of the overall teachings of the disclosure. Accordingly, theparticular arrangements disclosed are meant to be illustrative only andnot limiting as to the scope of invention.

What is claimed is:
 1. A syringe assembly, comprising: a syringe barrelhaving a first end, a second end, and a sidewall extending therebetweendefining a chamber; a stopper slideably disposed at least partiallywithin the chamber; and a plunger rod having an inner member engagedwith a portion of the stopper and an outer member adapted for rotationaladvancement with respect to the inner member to axially displace theouter member with respect to the inner member, wherein the plunger rodis transitionable from a collapsed position in which a portion of theinner member is nested within the outer member, to an extended positionin which the same portion of the inner member extends outside the outermember.
 2. The syringe assembly of claim 1, wherein the inner membercomprises a radial extension and the outer member defines a trackadapted to receive the radial extension therein.
 3. The syringe assemblyof claim 2, wherein the track is at least partially helical about anouter surface of the outer member.
 4. The syringe assembly of claim 2,wherein the radial extension remains substantially stationary duringtransition of the plunger rod from the collapsed position to theextended position.
 5. The syringe assembly of claim 4, wherein the outermember is rotated about the inner member to axially displace the outermember with respect to the inner member.
 6. The syringe assembly ofclaim 2, wherein the track extends between a proximal end and a distalend, the distal end comprising a restraint for locking the radialextension therein in the extended position.
 7. The syringe assembly ofclaim 1, wherein the stopper remains substantially stationary duringtransition of the plunger rod from the collapsed position to theextended position.
 8. The syringe assembly of claim 1, furthercomprising a medication or drug disposed within the chamber.
 9. Aplunger rod assembly comprising a plunger rod for use with a syringeassembly, the plunger rod comprising: an inner member having a distalend configured for securement to a stopper disposed within a syringebarrel; an outer member having an open portion configured for rotationaladvancement with respect to the inner member to axially displace theouter member with respect to the inner member, wherein the plunger rodis transitionable from a collapsed position in which a portion of theinner member is nested within the outer member, to an extended positionin which the same portion of the inner member extends outside the outermember; and a restraint configured to limit axial advancement of theouter member with respect to the inner member in the extended position.10. The plunger rod assembly of claim 9, wherein the restraint isconfigured to limit axial advancement of the outer member in both aproximal direction and a distal direction in the extended position. 11.The plunger rod assembly of claim 9, wherein the inner member comprisesa radial extension and the outer member defines a track adapted toreceive the radial extension therein.
 12. The plunger rod assembly ofclaim 11, wherein the track is at least partially helical about an outersurface of the outer member.
 13. The plunger rod assembly of claim 11,wherein the radial extension remains substantially stationary duringtransition of the plunger rod from the collapsed position to theextended position.
 14. The plunger rod assembly of claim 11, wherein thetrack extends between a proximal end and a distal end, the distal endcomprising the restraint wherein the restraint locks the radialextension therein in the extended position.
 15. A syringe assembly,comprising: a syringe barrel having a first end, a second end, and asidewall extending therebetween defiling a chamber; a stopper slideablydisposed at least partially within the chamber; and a plunger rodcomprising: an inner member engaged with a portion of the stopper andcomprising a radial extension; and an outer member defining a trackadapted to receive the radial extension therein, wherein rotation of theouter member about the inner member axially displaces the track aboutthe radial extension to transition the plunger rod from a collapsedposition in which a portion of the inner member is nested within theouter member, to an extended position in which the same portion of theinner member extends outside the outer member.
 16. The syringe assemblyof claim 15, wherein the track is at least partially helical about anouter surface of the outer member.
 17. The syringe assembly of claim 15,wherein an initial portion of the inner member and an initial portion ofthe outer member are disposed within the syringe barrel in the collapsedposition.
 18. The syringe assembly of claim 17, wherein the initialportion of the outer member is external to the syringe barrel in theextended position.
 19. The syringe assembly of claim 15, wherein thetrack extends between a proximal end and a distal end, the distal endcomprising a restraint for locking the radial extension therein in theextended position.
 20. The syringe assembly of claim 15, furthercomprising a medication or a drug disposed within the chamber of thesyringe barrel.